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Merlin: Computer-Aided Oligonucleotide Design for Large Scale Genome Engineering with MAGE.
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Efficient selection of unique and popular oligos for large EST databases.
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Targeted sequencing of large genomic regions with CATCH-Seq.
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CRAMER: a lightweight, highly customizable web-based genome browser supporting multiple visualization instances.
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The Human OligoGenome Resource: a database of oligonucleotide capture probes for resequencing target regions across the human genome.
Nucleic Acids Res. 2012 Jan;40(Database issue):D1137-43. doi: 10.1093/nar/gkr973. Epub 2011 Nov 18.

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OLTA: Optimizing bait seLection for TArgeted sequencing.
Bioinformatics. 2025 Mar 29;41(4). doi: 10.1093/bioinformatics/btaf146.
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Syotti: scalable bait design for DNA enrichment.
Bioinformatics. 2022 Jun 24;38(Suppl 1):i177-i184. doi: 10.1093/bioinformatics/btac226.
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Accurate long-read sequencing allows assembly of the duplicated RHD and RHCE genes harboring variants relevant to blood transfusion.
Am J Hum Genet. 2022 Jan 6;109(1):180-191. doi: 10.1016/j.ajhg.2021.12.003. Epub 2021 Dec 29.
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FISH Going Meso-Scale: A Microscopic Search for Chromatin Domains.
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本文引用的文献

1
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome.
Nat Biotechnol. 2019 Oct;37(10):1155-1162. doi: 10.1038/s41587-019-0217-9. Epub 2019 Aug 12.
2
iFISH is a publically available resource enabling versatile DNA FISH to study genome architecture.
Nat Commun. 2019 Apr 9;10(1):1636. doi: 10.1038/s41467-019-09616-w.
3
OligoMiner provides a rapid, flexible environment for the design of genome-scale oligonucleotide in situ hybridization probes.
Proc Natl Acad Sci U S A. 2018 Mar 6;115(10):E2183-E2192. doi: 10.1073/pnas.1714530115. Epub 2018 Feb 20.
4
Primer3_masker: integrating masking of template sequence with primer design software.
Bioinformatics. 2018 Jun 1;34(11):1937-1938. doi: 10.1093/bioinformatics/bty036.
5
ThermoAlign: a genome-aware primer design tool for tiled amplicon resequencing.
Sci Rep. 2017 Mar 16;7:44437. doi: 10.1038/srep44437.
6
MPD: multiplex primer design for next-generation targeted sequencing.
BMC Bioinformatics. 2017 Jan 5;18(1):14. doi: 10.1186/s12859-016-1453-3.
8
Haplotyping germline and cancer genomes with high-throughput linked-read sequencing.
Nat Biotechnol. 2016 Mar;34(3):303-11. doi: 10.1038/nbt.3432. Epub 2016 Feb 1.
9
Dealing with pseudogenes in molecular diagnostics in the next-generation sequencing era.
Methods Mol Biol. 2014;1167:303-15. doi: 10.1007/978-1-4939-0835-6_21.
10
BOND: Basic OligoNucleotide Design.
BMC Bioinformatics. 2013 Feb 27;14:69. doi: 10.1186/1471-2105-14-69.

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